Special

RnoINT0138576 @ rn6

Intron Retention

Gene
Description
solute carrier family 4 member 8 [Source:RGD Symbol;Acc:735164]
Coordinates
chr7:142454723-142457145:+
Coord C1 exon
chr7:142454723-142454974
Coord A exon
chr7:142454975-142457076
Coord C2 exon
chr7:142457077-142457145
Length
2102 bp
Sequences
Splice sites
5' ss Seq
AAGGTATTC
5' ss Score
6.8
3' ss Seq
CCTTGAGTCTTTCTCTGCAGTTT
3' ss Score
7.27
Exon sequences
Seq C1 exon
AAAGGCTGTGGCTACCATCTGGACCTGCTCGTGGTGGCCATCATGCTGGGGGTCTGCTCCCTCATGGGCCTGCCTTGGTTCGTGGCTGCGACCGTGCTGTCCATTACTCATGTGAATAGCCTCAAGCTGGAATCTGAATGCTCTGCTCCGGGGGAGCAGCCTAAGTTTCTGGGCATCCGAGAACAGAGAGTCACGGGCCTCATGATCTTTGTGCTGATGGGCTGCTCCGTCTTCATGACAGCGGTCTTAAAG
Seq A exon
GTATTCCTTCACTAGCAACGCGGACGGCCTCTGTGCGGGGAATGCAGTGGCCAGTGTATATACACACACAGAGGCATGCCCTGGAAGAAGTTGTTCTTGTGGACAGTTAAGTGTGCTTAAGAAATGGACATGATAGTAATAGAATGTGATAAGTGATCCAAAGGTCCGCCGCCATTTTCCTTTCTCTGGATAGCTCCCTTTATGCTGGAAGGCTGAGCCTTCAACATGCAAAGCAGGCAGTGCAGGGCTGAGCTCTGCCCCGCCCCTTTTTACCCTGAGGTTGTTTTTGAGAAGTTCTTATGCAGTTCTGGCTGGTGTAAAAATCACTATGTGAGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGATTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAGAATCAAAAAAAAAAAACCAAAAAACAAAACAAAACAAAAAAAAACACTACGTGACTAGGCTGGCTTTGAACCTGCAACAGTCATACTGTCTCTAAGTTTTGGTTGCTAGGATCATAAATATTGTTCCTGTTTGGTTTCGGTTGTGTGGTAAGGATCATGACCAAAAGCAACCTGGGGAGGAAAGGGTTACTTTACCTTGTACTTTCAGGAAACAGTCAATCCTGAAGGAAAGTCAGGGGGGGTGGGGCTCGAGCGGGTGGGGCCTCACCAGGTACCTGCTCTCAACTCCACCTGCTCAGATAACTTTGTTCTACAATGCAGGGCCACCTGCCTAGCAGGGGTGCTGCCCAGGGCACTGGCCCTCCCACATTAATCAAGGCAGTGTTCCCCAGACAGTCCTCAGCTGAAGTTTCCTCTTTTCAGGGGACTCCTAAGTTGGGTCACATTGGTCATGAAGACTCACTCAGCAGCACACTGTCCAACAGTGCTGCACACCTGTCACCAAACAGAAATGTCCAGCTACCTAGAGTCGGGGCAACATAGTCCAGTGTGGCCTTTCTAACTCTGAGAGAAAGGATGTTGTCCTTTAGCCCAGGATGAGAGCGTGTGAGGGGCTAGGCTTGTGGAACAGCACCAGGCTCTGGGTGGGCTCCTCAGAACTGTGGCAGCCAGGCAGGTGGCGCACGTGGATGGAGGTAGGAAGAGCAGAAGTTCAAGGCCATCCTCAGGACCTTCTTTGTGTACACACCGAGTTCGAGGCCAGCCAGGGGAACAAACAACAGAAACCGAGTTCAGTCTTGAGCCGGGACCCTCTAGACTGGCTTTGGAGGCCTGTTTCTCACGCTCACACTTGCATGAAGATTTTCTCTAAGGTGAACACATGTGACAGCGAAGCCATGTTCACACGCCTATGGACACTTTAAAAAGCGCAGCATAACAACATGTTCCCAACTCACTTCCTCTCCACTGCCCTCAAGTCTCAGGTCAGAAAGCAGGAATTATTTTTAGTCTGTGTCAAAATGCACAAAGCTCCAAAGGATGCGATAATTATAGAAAGATTTAAATTATGTCTGTGAAGTCTATGTGCACGTGTGTGCATGTGTGTGTGTGCGTGTACATGCACAGATGGGTGTGAGTGTATGTGTGTCCCCATCTGTCTACTCATAATCTAGGGAGGAGACATAAGGCCTATGACTTACCTTATTTCAGCAACTTCATTTCAGAACAAAATGACTTCGATGTTACCAGAGCATGGGGTTTTCCAAGATAACTGAAGGAGAGGCAGCAGAAACAAAGACCGTGTTTATGAGACTGTGGCTTTGTTTCATTTTTGGAATTAAACATTTATATAGATGGGACGTAGTGGTGTACACCTTTAGTCCCAGCACTCAGGATGCAGAGATGGGCAGGTGTCCATGAGTTCAGGACAAGCCTAGCCTACATAGTGAGTTCTAAGCAAGACCCTGTGTCAATACTGCTAGACTTCAGTGCTGCTGGGATTGCCACAGCATGGGATCCTACCCACCTGTGCACACACACACACACACATCCATACACCTGTGGCCACGTGTGCACGCACATGCACACATTCCCGGTCATGTGCACGCTCGTGGTTCTGTGCACACACACGTGGACATAGACTTTACAGCCCTAATTTAAATCTTACCTTGAGTCTTTCTCTGCAG
Seq C2 exon
TTTATCCCAATGCCAGTGCTCTACGGAGTTTTCCTCTACATGGGAGTCTCTTCTCTACAAGGAATCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000028879:ENSRNOT00000040890:19
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0095516=HCO3_cotransp=FE(16.1=100)
A:
NA
C2:
PF0095516=HCO3_cotransp=FE(4.3=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]